基于证据推理与模型认知的有机物分子结构探究——以“三谱解析阿司匹林”为例

为了反映化学学科发展的特点和趋势,充分突显现代科学技术发展的新成就。以“三谱解析阿司匹林”的4个教学环节为例,着重阐述质谱、红外光谱、核磁共振氢谱在有机物分子结构探究教学中的运用策略,从而建构出探究有机物分子结构的一般模型,培养学生的证据推理与模型认知的化学核心素养。     

探究型课堂教学中教师“放手”与“引导”的艺术

正探究型教学是课堂教学的重要形式,也是提升学生学科核心素养的有效方式,在落实时,教师需要处理好"放手"与"引导"之间的关系。1探究型教学的现状在新课改的引领下,教师的探究型教学走向了两个极端:有些形似探究的课堂活动,其实是在教师"严密布局"中展开的,造成了教师"放手"而学生实则被动探究的假象,这是换一种表现形式的"灌输式"教学;有些教师将课堂全部交予学生,没有任何方法与情境设定,从而导致课堂教学效率低下,部分能力相对较差的学生,整节课都处于无序的状态下,形成了教师"放手"而学生实则无效探究的状态。     

“原电池”的项目式教学*——探究“水动力”盐水灯发光之谜

以“菲律宾能源救星”创设探究情境,以“水动力”盐水灯发光之谜展开项目式学习探究设计之旅,在项目任务推进中对“水动力”盐水灯的原理和影响因素展开深入探究,重建学生对原电池的模型认知;设计并制作“家庭版”水动力灯,最终回归到指导抗震减灾等社会场景中去,加强学科与真实情境的结合与应用,锻炼和提升学生的科学精神与社会责任感,发展学生的化学学科核心素养。     

化学课堂探究教学“制订计划”的评价

为了解化学课堂探究教学“制订计划”的有效性,在课堂观察与分析的基础上,提出化学课堂探究教学“制订计划”系统分析量表,并结合具体化学课堂探究教学,从计划制订的主体、计划制订的过程、计划内容本身等3个方面解析了“制订计划”环节。结果启示：化学课堂探究教学“制订计划”系统分析量表能科学有效地指导化学课堂探究教学,特别是其“制订计划”的设计、实施与评价。     

“燃烧条件”探究实验的创新改进

对人教版九年级化学上册第七单元的“燃烧条件”探究实验进行了改进。引入了水浴加热、温度传感器、氮气氛围保护、便携氧气瓶等创新点,改进的实验具有高效性、科学性、环保性。     

促进学生“科学探究与创新意识”素养的发展*——以“氢氧化亚铁的制备”为例

以“氢氧化亚铁的制备”教学设计为例,通过开展专题课,引导学生深入探究氢氧化亚铁制备实验的设计与改进,重点关注学生“科学探究与创新意识”素养水平的发展,并基于具体的测评数据进行反馈评价。     

自主探究交互软件在“物质的量”教学中的应用

探讨了"物质的量"教学中存在的主要问题,提出应用自主探究的交互教学软件,以探究活动为依托,以培养学生科学研究方法和逻辑推理能力为主旨,从学生已有的知识和经验出发,通过具体的可理解和可操作的问题入手,形成任务并在任务驱动下实现学生自主探究,得到结论、建立概念和导出公式。实践表明,该方法能有效帮助学生建立有关摩尔的概念和计算公式,消除对概念的迷茫,并在定量科学研究方法培养中有一定的作用。     

基于“教学评一体化”的化学探究活动一般思路方法建构*——以“物质的分离与提纯”复习课为例

针对学生面对化学实验探究问题无从下手的情况,以物质的分离与提纯这一类探究实验为例,通过“教学评一体化”的教学模式引导学生建立解决“物质分离与提纯”探究实验的一般思路方法。     

“素养为本”的化学课堂教学*——以“原子晶体”为例

基于“素养为本”视角,以“原子晶体”的教学为例,对教学主题内容、教学现状及学情进行分析;以发展学生化学学科核心素养为主旨确定教学目标;以“微粒-微粒间的相互作用-物质的聚集状态-物质性质”的认识思路为主线,以“模型认知,建构概念-证据推理,归纳性质-微观探析,探究结构-科学史实,揭示价值”的任务型教学流程,达到落实并发展学生化学学科核心素养的目的。     

促进“深度学习”的教学实践与思考——以“基于桃酥烘焙配方的实验探究”为例

以“基于桃酥烘培配方的实验探究”单元课的设计与实施为例,从情境素材的选取、课堂问题的设计、课堂任务的确定、学习活动的设计、持续性评价方案的设计等方面论述了促进“深度学习”教学的生成过程。     

Di­methyl­phenyl­sulfonium tri­fluoro­methane­sulfonate and methyl­di­phenyl­sulfonium tri­fluoro­methane­sulfonate

The bonding geometry of sulfur in the cations of the title compounds, C₈H₁₁S⁺·CF₃SO₃^? and C₁₃H₁₃S⁺·CF₃SO₃^?, respectively, is similar and is independent of the ratio of the Me/Ph substituents. As expected, in both cations, the S—Ph bonds are somewhat shorter than the S—Me bonds. In both crystal structures, the interaction between cations and anions is similar.     

Bis(μ‐hexa­methyl­enetetr­amine)­bis(aqua­di­bromo­cadmium)­di­aqua­di­bromo­cadmium dihydrate

The title compound, poly­[[di­aqua­di­bromo­cadmium‐μ‐(1,3,5,7‐tetra­aza­tri­cyclo[3.3.1.1^3,7]decane‐N¹:N⁵)‐aqua­cad­mium‐di‐μ‐bromo‐aqua­cadmium‐μ‐(1,3,5,7‐tetra­aza­tri­cyclo[3.3.1.1^3,7]decane‐N¹:N⁵)‐di‐μ‐bromo] dihydrate], [Cd₃­Br₆­(C₆­H₁₂­N₄)₂­(H₂O)₄]·­2H₂O, is made up of two‐dimensional neutral rectangular coordination layers. Each rectangular subunit is enclosed by a pair of Cd₃(μ₂‐Br)₆(H₂O)₃ fragments and a pair of (μ₂‐hmt)Cd(H₂O)₂Br₂(μ₂‐hmt) fragments as sides (hmt is hexa­methyl­enetetr­amine). The unique Cd^II atom in the Cd₂Br₂ ring in the Cd₃(μ₂‐Br)₆(H₂O)₃ fragment is in a slightly distorted octahedral CdNOBr₄ geometry, surrounded by one hmt ligand [2.433 (5) Å], one aqua ligand [2.273 (4) Å] and four Br atoms [2.6409 (11)–3.0270 (14) Å]. The Cd^II atom in the (μ₂‐hmt)Cd(H₂O)₂Br₂(μ₂‐hmt) fragment lies on an inversion center and is in a highly distorted octahedral CdN₂O₂Br₂ geometry, surrounded by two trans‐related N atoms of two hmt ligands [2.479 (5) Å], two trans‐related aqua ligands [2.294 (4) Å] and two trans‐related Br atoms [2.6755 (12) Å]. Adjacent two‐dimensional coordination sheets are connected into a three‐dimensional network by hydrogen bonds involving lattice water mol­ecules, and the aqua, bromo and hmt ligands belonging to different layers.     

Specific heat on Sr<Subscript>2</Subscript>Nb<Subscript>2</Subscript>O<Subscript>7</Subscript> and Sr<Subscript>2</Subscript>Ta<Subscript>2</Subscript>O<Subscript>7</Subscript>

Summary Specific heats on the single crystals of Sr₂Nb₂O₇, Sr₂Ta₂O₇ and (Sr_1-xBa_x)₂Nb₂O₇ were measured in a wide temperature range of 2-600 K. Heat anomalies of a λ-type were observed at the incommensurate phase transition of T_INC (=495 K) on Sr₂Nb₂O₇ and at the super-lattice phase transition of T_SL (=443 K) on Sr₂Ta₂O₇; the transition enthalpies and the transition entropies were estimated. Furthermore, a small heat anomaly was observed at the low temperature ferroelectric phase transition of T_LOW (=95 K) on Sr₂Nb₂O₇. The transition temperature T_LOW decreases with increasing Ba content x and it vanishes for samples of x>2%.     

2,4‐Di­nitro­phenyl­hydrazones of 2,4‐di­hydroxy­benz­aldehyde, 2,4‐di­hydroxy­aceto­phenone and 2,4‐di­hydroxy­benzo­phenone

In 2,4‐di­hydroxy­benz­aldehyde 2,4‐di­nitro­phenyl­hydrazone N,N‐di­methyl­form­amide solvate {or 4‐[(2,4‐di­nitro­phenyl)­hydrazono­methyl]­benzene‐1,3‐diol N,N‐di­methyl­form­amide solvate}, C₁₃H₁₀N₄O₆·C₃H₇NO, (X), 2,4‐di­hydroxy­aceto­phenone 2,4‐di­nitro­phenyl­hydrazone N,N‐di­methyl­form­am­ide solvate (or 4‐{1‐[(2,4‐di­nitro­phenyl)hydrazono]ethyl}benzene‐1,3‐diol N,N‐di­methyl­form­amide solvate), C₁₄H₁₂N₄O₆·C₃H₇NO, (XI), and 2,4‐di­hydroxy­benzo­phenone 2,4‐di­nitro­phenyl­hydrazone N,N‐di­methyl­acet­amide solvate (or 4‐­{[(2,4‐di­nitro­phenyl)hydrazono]phenyl­methyl}benzene‐1,3‐diol N,N‐di­methyl­acet­amide solvate), C₁₉H₁₄N₄O₆·C₄H₉NO, (XII), the molecules all lack a center of symmetry, crystallize in centrosymmetric space groups and have been observed to exhibit non‐linear optical activity. In each case, the hydrazone skeleton is fairly planar, facilitated by the presence of two intramolecular hydrogen bonds and some partial N—N double‐bond character. Each molecule is hydrogen bonded to one solvent mol­ecule.     

Tetra­phenyl­phos­phonium 4‐hydroxy‐2,2,6,6‐tetra­methyl­piperidinyl­oxy‐4‐sulfonate

The title compound, C₂₄H₂₀P⁺·C₉H₁₇NO₅S⁻, consists of an organic monovalent cation and an organic monovalent anion, the latter being derived from the TEMPO radical (TEMPO is 2,2,6,6‐tetra­methyl­piperidin‐1‐oxyl). Two inversion‐related anions interact via two –O—H⃛O—S– hydrogen bonds, forming a dimer in which there are no short contacts between the spin centres (–N—O) of the TEMPO(OH)SO₃⁻ anions. Furthermore, no significant magnetic interaction is observed between the dimers because the dimer is surrounded by cations. These results are consistent with the paramagnetic behaviour of the title salt.     

9,10‐Di­phenyl‐9,10‐epi­dioxy­anthra­cene and 9,10‐di­hydro‐10,10‐di­methoxy‐9‐phenyl­anthracen‐9‐ol

9,10‐Di­phenyl‐9,10‐epi­dioxy­anthracene, C₂₆H₁₈O₂, (I), was accidentally used in a photo­oxy­genation reaction that produced 9,10‐di­hydro‐10,10‐di­methoxy‐9‐phenyl­anthracen‐9‐ol, C₂₂H₂₀O₃, (II). In both compounds, the phenyl rings are approximately orthogonal to the anthracene moiety. The conformation of the anthracene moiety differs as a result of substitution. Intramolecular C—H⃛O interactions in (I) form two approximately planar S(5) rings in each of the two crystallographically independent mol­ecules. The packing of (I) and (II) consists of molecular dimers stabilized by C—H⃛O interactions and of molecular chains stabilized by O—H⃛O interactions, respectively.     

Chemical durability of MoO<Subscript>3</Subscript>-P<Subscript>2</Subscript>O<Subscript>5</Subscript> and K<Subscript>2</Subscript>O-MoO<Subscript>3</Subscript>-P<Subscript>2</Subscript>O<Subscript>5</Subscript> glasses

Thermal and chemical durability studies of the phosphate glasses belonging to the binary MoO₃-P₂O₅ and the ternary K₂O-MoO₃-P₂O₅ systems are reported. The chemical resistant attack tests carried out on the free alkaline MoO₃-P₂O₅ glasses show that the glass associated with the P/Mo ratio 2 has the high chemical durability. It shows also a high glass transition temperature value. The above findings are interpreted in terms of the cross-link density of the glasses and the strength of the M-O bonds (M=P, Mo). The influence of K₂O addition on the properties (density, T _g, durability) of this binary high water resistant glass is studied. It is found that the chemical durability along with the other physical properties are reduced by the incroporation of K₂O in the glass matrix. The results were explained by assuming the formation of non-bridging oxygens and weak bonds. The mechanism of the dissolution of these glasses is proposed.     

Thermal analysis study of Bi<Subscript>2</Subscript>Sr<Subscript>2</Subscript>Ca<Subscript>2</Subscript>Cu<Subscript>3-x</Subscript>Er<Subscript>x</Subscript>O<Subscript>10+δ</Subscript> glass-ceramic system

Summary We have fabricated glasses in the Bi-2223 HT_c superconductor system with Bi₂Sr₂Ca₂Cu_3-xEr_xO_{10+ δ} nominal composition, where x=0.5 and 1.0, by the glass-ceramic technique. Using an analysis developed for non-isothermal crystallization studies, information on some aspects of crystallization temperature and thermal properties has been obtained. The crystallization studies were made using DTA with several uniform rates. The calculations of crystallization activation energies, E_a, and the Avrami parameters, n, were made based on the non-isothermal kinetic theory of Kissinger and the Ozawa’s equations. The DTA data of the samples showed that the first crystallization temperature, T_x1, increases and the second crystallization temperature, T_x2, decreases by increasing the Er concentration. This suggests that the Er substitution had significant effect on the glassification of the BSCCO material due to change on the surface nucleation and increased ionic activities at high temperature region. The activation energy for crystallization, E_a, of the samples was also showed an increase at high Er concentration case. However, the Avrami parameter, n, decreased from 2.5 to 1.7 for x=0.5 and 1.0 samples, respectively. This suggests that the growth mechanism is diffusion-controlled and three-dimensional parabolic growth takes place near the first crystallization temperature. The oxidization rates and the activation barrier for oxygen out-diffusion process, E, was calculated using the TG data. It was found that the total mass gain in the x=0.5 sample is comparably smaller than that of the x=1.0 sample. This shows that the oxygen absorption of the x=1.0 sample is faster than the x=0.5 sample, leading to increase in the oxidization rate in the x=1.0 material.     

Methyl­tri­phenyl­stibonium tetra­fluoro­borate

In the title compound, [Sb(CH₃)(C₆H₅)₃]BF₄, there are four independent cations and anions in the asymmetric unit. The geometry around the Sb atom is distorted tetrahedral, with Sb—C distances in the range 2.077 (4)–2.099 (10) Å and angles at the Sb atom in the range 103.3 (3)–119.0 (4)°.